world-record SVG rate under 1 sun was 4.0 kg m −2 h −1 , which was achieved in a hydrophilic hydrogel evaporator with hydrophobic island-shaped patches. [25] Unfortunately, affected by seasons or regions, the outdoor sunlight intensity is usually far lower than 1 sun, [10,17,23,27] and the reported evaporators showed much lower vapor yields under weaker natural sunlight conditions. [17,19,23] Thus developing evaporators with high vapor yields under weaker solar irradiations is expected for practical applications. Meanwhile, the fundamental evaporation mechanisms at the evaporator interface have rarely been studied, [25] which will conduct the reasonable design of the evaporator structure with high SVG performance. Inspired by previous work about increased-up water flux in the confined hydrophobic nanochannels, [28,29] we designed nanoconfined water molecule channels (NCWMCs) to achieve high-yield SVG under weaker sunlight. Here, we synthesized a 1D-O-doped MoS 2−x nanosheets assembly (1D-OMoSNSA) via a one-pot solvothermal approach. In the structure of 1D-OMo-SNSA, the gaps formed during stacking were conducive to rapid water transport, and the NCWMC of 3.5 nm spacing between ultrathin O-MoS 2−x nanosheets could reduce water vaporization enthalpy by facilitating water molecules to evaporate as clusters. After heat loss management, this evaporator showed the SVG rate of 2.50 kg m −2 h −1 under 1 sun with the energy efficiency of 89.6%. Furthermore, under weaker natural sunlight irradiation (0.5 sun), the SVG rate could reach 1.25 kg m −2 h −1 , which exceeded the highest reported value, [23] and was comparable with most reported vapor yields at 1 sun. [6-11,13-15,17,19] Molecular dynamics (MD) simulations revealed that this unique performance could be ascribed to the cluster-evaporation process in the NCWMC system. This evaporator was further applied for the practical water purification procedure, and exhibited excellent performance in both seawater desalination and wastewater treatment. The 1D-OMoSNSA was prepared via a simple one-pot solvothermal approach, in which ammonium heptamolybdate (AHM) and thiourea were used as precursors, and oleylamine was used as surfactant. In a typical synthesized process, AHM and thiourea were first dissolved in deionized water, followed by mixed with terpineol and oleylamine. The mixture was sealed in an autoclave and heated at 200 °C for 6 h, and the product was washed by ethanol (for the detailed synthesized process, see Experimental Section). Figure 1a showed the powder X-ray diffraction (XRD) pattern of the prepared product. Compared with